US9090696B2ActiveUtilityA1
Polynucleotides encoding anti-CD40 antibodies
Est. expiryMar 31, 2030(~3.7 yrs left)· nominal 20-yr term from priority
A61P 7/06A61P 37/02A61P 7/10A61P 7/00A61P 9/00A61P 35/00A61P 3/10A61P 39/00A61P 7/04A61P 37/06A61P 5/00A61P 37/00A61P 43/00A61P 25/00A61P 29/00A61P 27/00A61P 3/00A61P 15/12A61P 17/00A61P 17/06A61P 15/00A61P 1/04A61P 19/04A61P 1/16A61P 21/00A61P 21/04A61P 1/00A61P 13/12C07K 2317/92C07K 2317/76C07K 2317/53A61K 2039/505C07K 2317/73C07K 2317/565C07K 1/22C07K 2317/24C07K 2317/515C07K 2317/732C07K 2317/51C07K 2317/94C07K 2317/33C07K 16/2878C07K 2317/71A61K 9/0019C07K 14/475A61K 38/17A61K 38/18A61K 39/395C07K 16/18C07K 14/435A61K 47/42C07K 16/28C07K 16/22A61K 49/16A61K 48/00
95
PatentIndex Score
33
Cited by
36
References
4
Claims
Abstract
The present invention relates to new humanized antagonistic anti-CD40 antibodies and therapeutic and diagnostic methods and compositions for using the same.
Claims
exact text as granted — not AI-modifiedThe invention claimed is:
1. An isolated polynucleotide encoding a humanized monoclonal antibody or antibody fragment that specifically binds to human CD40 having a heavy chain variable region amino acid sequence and a light chain variable region amino acid sequence, wherein the heavy chain variable region amino acid sequence comprises any of SEQ ID NO: 1 to 4, SEQ ID NO:27, SEQ ID NO:28, SEQ ID NO: 29, SEQ ID NO:30, SEQ ID NO:32, SEQ ID NO:33, SEQ ID NO:34, SEQ ID NO:35, SEQ ID NO:37, SEQ ID NO:38, SEQ ID NO:39, SEQ ID NO: 40, SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID. NO. 50, SEQ ID NO: 53, SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 72, or SEQ ID NO: 73; and light chain variable region amino acid sequence comprises any of SEQ ID NO: 5 to SEQ ID NO:8, SEQ ID NO:26, SEQ ID NO:31, SEQ ID NO:36, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:50, SEQ ID NO:51, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:55, SEQ ID NO:56, SEQ ID NO:74, SEQ ID NO:75, or SEQ ID NO:76.
2. The polynucleotide of claim 1 , wherein the heavy chain variable region amino acid sequence comprises any of SEQ ID NO:27, SEQ ID NO:28, SEQ ID NO: 29, SEQ ID NO:30, SEQ ID NO:32, SEQ ID NO:33, SEQ ID NO:34, SEQ ID NO:35, SEQ ID NO:37, SEQ ID NO:38, SEQ ID NO:39, or SEQ ID NO: 40; and the light chain variable region amino acid sequence comprises any of SEQ ID NO:26, SEQ ID NO:31, or SEQ ID NO:36.
3. The polynucleotide of claim 1 , wherein the heavy chain variable region amino acid sequence comprises any of SEQ ID NO: 42, SEQ ID NO: 44, SEQ ID NO: 46, SEQ ID NO: 48, SEQ ID. NO. 50, SEQ ID NO: 53, SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 72, or SEQ ID NO: 73; and the light chain variable region amino acid sequence comprises any of SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:50, SEQ ID NO:51, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:55, SEQ ID NO:56, SEQ ID NO:74, SEQ ID NO:75, or SEQ ID NO:76.
4. The polynucleotide of claim 1 , wherein the heavy chain variable region amino acid sequence and the light chain variable amino acid sequence are selected from the group consisting of SEQ ID NO:27 and SEQ ID NO:26, respectively; SEQ ID NO:28 and SEQ ID NO:26, respectively; SEQ ID NO:29 and SEQ ID NO:26, respectively; SEQ ID NO:30 and SEQ ID NO:26, respectively; SEQ ID NO:32 and SEQ ID NO:31, respectively; SEQ ID NO:33 and SEQ ID NO:31, respectively; SEQ ID NO:34 and SEQ ID NO:31, respectively; SEQ ID NO:35 and SEQ ID NO:31, respectively; SEQ ID NO:37 and SEQ ID NO:36, respectively; SEQ ID NO:38 and SEQ ID NO:36, respectively; SEQ ID NO:39 and SEQ ID NO:36, respectively; SEQ ID NO:40 and SEQ ID NO: 36, respectively.Cited by (0)
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